ENST00000369846.9:c.1231+16T>G
MANE Select
|
ENSP00000358861.4:n.1231+16T>G
|
|
ENST00000369846.8:c.1231+16T>G
|
ENSP00000358861.4:n.1231+16T>G
|
|
ENST00000392959.5:c.1231+16T>G
|
ENSP00000376686.1:n.1231+16T>G
|
|
ENST00000467898.3:c.1247T>G
|
ENSP00000474463.1:p.Leu416Trp
|
|
NM_001122769.2:c.1231+16T>G
|
NP_001116241.1:n.1231+16T>G
|
|
NM_181714.3:c.1231+16T>G
|
NP_859065.2:n.1231+16T>G
|
|
XM_005248665.3:c.1231+16T>G
|
XP_005248722.1:n.1231+16T>G
|
|
XM_011535504.1:c.1231+16T>G
|
XP_011533806.1:n.1231+16T>G
|
|
XR_942715.1:n.1179A>C
|
|
|
XR_942716.1:n.1141A>C
|
|
|
XR_942717.1:n.1413A>C
|
|
|
XM_005248665.4:c.1231+16T>G
|
XP_005248722.1:n.1231+16T>G
|
|
XR_001744213.1:n.2804A>C
|
|
|
XR_001744214.1:n.2766A>C
|
|
|
NM_001122769.3:c.1231+16T>G
MANE Select
|
NP_001116241.1:n.1231+16T>G
|
|
NM_181714.4:c.1231+16T>G
|
NP_859065.2:n.1231+16T>G
|
|